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$33 per hour
...of experience in quality testing, strong problem-solving skills, and excellent communication abilities. You will ensure compliance with GMP standards and document quality control findings. This is a contract position offering a pay rate of $33.00/hr. #J-18808-Ljbffr...SuggestedContract work- ...Maker's Pride is seeking a Quality Lead to serve as the on-shift QA contact when supervision isn’t available and to manage FSQA programs... .... You will lead QA activities on a shift basis and ensure GMP compliance. Responsibilities include auditing, incident report oversight...SuggestedShift work
- ...Engineering Lead to oversee global engineering programs, ensuring GMP compliance, contamination control, and product quality across... ...manufacturing and medical devices. You will act as the primary QA representative on cross-functional teams and drive risk-based decisions...Suggested
- ...Summary: The Operational Area Senior Quality Specialist will provide QA support of manufacturing operations, analytical laboratory... ...and experience Experience providing QA support and oversight of GMP manufacturing operation Experience successfully leading event investigations...SuggestedWork at office
- ...Vertex Pharmaceuticals in Boston seeks a GMP QA Analytical Sr. Quality Specialist to serve as a subject matter expert in QA and compliance for the Analytical function. The role supports clinical and commercial programs and collaborates across teams to ensure rapid, accurate...Suggested
- ...Key Responsibilities: Lead sponsor-side QA oversight of CMOs across pre-clinical, clinical, and commercial manufacturing — drug... ...Development Maintain quality metrics and periodically revise GMP SOPs Qualifications: ~ Bachelor's degree in a scientific...Suggested
- ...Croda, a global life sciences company based in Alabama, is seeking a Lead QA Specialist to own document control for GMP and QA activities at the Alabaster site. You will manage batch records, SOPs, CAPA investigations, data analysis and prepare for customer and FDA audits...Suggested
- ...Bachem Americas is seeking a Sr. Quality Assurance Specialist to strengthen GMP compliance across manufacturing and QC operations in Vista, CA. You will review GMP documents, support real-time batch record review, lead audits, and drive LEAN GMP improvements with cross...Suggested
$50 - $54 per hour
...Akraya, Inc. in Greenville, NC is seeking a Quality Specialist for sterile manufacturing to uphold GMP standards and ensure regulatory compliance for commercial products and development services. You will lead investigations of deviations, guide aseptic techniques on...SuggestedHourly pay- ...Technical to provide technical quality guidance across contract manufacturing, testing, storage, and distribution. You will lead GMP QA functions, oversee CSPs through Phase 3, manage validation efforts, and drive CAPA, change control, and risk management while...SuggestedContract workRemote work
- ...Goodkind seeks a QA Supervisor to coordinate daily QA operations and lead QA personnel in a GMP-regulated manufacturing environment. You will ensure compliance with internal procedures and regulatory requirements while coordinating with Manufacturing, QC, and other departments...Suggested
- ...Excelsior Nutrition Inc. is seeking a QA Associate to inspect products at different development stages and ensure they meet set standards... ...maintain master formulas/BOMs, and handle ERP entries as part of GMP-compliant manufacturing and QA release processes. #J-18808-...Suggested
- ...Porte, TX is seeking a Quality Assurance Specialist III to support QA programs and coordinate cross-functional IPT meetings for batch... ...a master's). Strong attention to data integrity, compliance with GMP, and teamwork are essential in this fast-paced environment; occasional...SuggestedShift work
- ...J.M. Murray Center, Inc. is seeking a Quality Assurance Manager in Cortland, NY to lead the QMS and ensure compliance with FDA, ISO, GMP, and related regulations. The role oversees cross-functional activities in operations, maintenance, and supply chain to drive continuous...Suggested
- Judo Bio is seeking a Director of Quality Assurance to lead GMP and quality systems across outsourced manufacturing and testing. The role... .... The candidate should bring 10+ years in pharma/biotech QA, strong GMP knowledge, and proven leadership to build scalable quality...Suggested
- ...Isotopes seeks an experienced Quality Assurance Specialist to support Ac-225 production at the Everett, WA facility. The role emphasizes GMP compliance, regulatory alignment with FDA 21 CFR 210/211 and ICH guidelines, radiation safety, and policy development. The successful...
- ...experienced Quality Assurance Associates to join their team in Kenosha County, Wisconsin. This role involves providing oversight for GMP operations, ensuring compliance with regulations, and supporting manufacturing activities on the night shift. Candidates will collaborate...Night shift
- ...Kdc One in New Jersey seeks a Quality Control Manager to lead QA/QC initiatives in cosmetics manufacturing. You will oversee inspections... ...testing, supplier quality, CAPA, and regulatory compliance with GMP, FDA, ISO standards, while driving continuous improvement. The...
- ...Job Summary The QA Senior Specialist will provide quality assurance support for pharmaceutical manufacturing operations, ensuring... ..., regulatory requirements, and Good Manufacturing Practices (GMP). The role will lead and coordinate quality projects across multiple...For contractors
$280k - $300k
...get it done, and have fun, seriously.POSITION SUMMARYThe Director, GMP Quality Assurance is responsible for the global oversight and... ...activities within the role’s scope.JOB FUNCTIONS/RESPONSIBILITIESProvide QA oversight of finished product (FP), from early development...Contract workLocal area$200k - $275k
...trials while providing phase-appropriate Good Manufacturing Practice (GMP) oversight for our drug substance (API) and drug product programs... ..., Informed Consent Forms, and Clinical Study Reports Provide QA oversight of external CMOs handling small molecule API synthesis,...Temporary work- ...products. You will perform and supervise microbial testing, maintain regulatory compliance, and contribute to continuous improvement in a GMP environment. The role emphasizes data integrity, training, troubleshooting and collaboration with multidisciplinary teams to...
- ...MillenniumSoft Inc is seeking a mid-level QA specialist to review Quality Notifications, complaints, deviations and related cGMP activities... ...ensuring documentation aligns with Quality Policies and FDA/GMP guidelines, conducting investigations, and contributing data for...
- ...Support in Massachusetts to provide routine quality oversight of GMP operations and real-time compliance support. You will review documents... ..., and collaborate with Manufacturing, Facilities, Engineering, QA, and Regulatory Affairs to ensure product quality and patient...
- ...materials in our Eddyville, Iowa lab. You will report results, support QA, and contribute to continuous improvement in a fast-paced... ...detail, teamwork, and knowledge of analytical chemistry, with familiarity in lab instrumentation and GMP guidelines. #J-18808-Ljbffr
- ...Ionis Pharmaceuticals, Inc. is seeking an Executive Director, GMP Quality to provide strategic leadership for GMP Quality activities across the Carlsbad campus and external sites. The role leads QA operations, regulatory inspections readiness, and collaboration with CMOs...
$94.6k - $141.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced technical resource... ..., including leadership of complex quality initiatives and QA oversight of external manufacturing operationsAt Vertex, we embrace...Full timeContract workSummer workRemote workFlexible hours2 days per week- ...material testing, data analysis, and quality compliance at 1 DNA Way, South San Francisco, CA. You will ensure testing activities meet GMP and regulatory standards, document results, and assist with investigations and root cause analysis. Ideal candidates have 0-5 years...
- ...and finished goods, document results, and ensure compliance with GMP, GDP, ISO and SOPs. You will manage holds and releases, perform rework... ...SAP and Excel to maintain daily reports, and collaborate with QA and production teams to sustain product integrity and customer...
- ...A GMP Quality Assurance Specialist is being sought for a 12-month contract in Boston to support clinical and commercial drug product... ...manufacturing operations. The ideal candidate has 5+ years of GMP QA experience in a cGMP environment, with 2-3 years for a Master’s...Contract workAfternoon shift


